# K111633: Aquilion LB Movement Base Kit

- Pathway: 510(k) (Traditional)
- Applicant: Toshiba America Medical Systems, In.C
- Decided: Aug 25, 2011 after 73 days
- Product code: JAK (System, X-Ray, Tomography, Computed)
- Device class: 2
- Regulation: 21 CFR 892.1750
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K903701 (1990). 5 ancestors in all.
4 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050458: TSX-201A Aquilion LB CT Scanner, Toshiba America Medical Systems, In.C (2005) Summary page 1.

## Most influential descendants
- K134025: Aquilion One Vision Self-Propelled Scan Base Kit for Ivr-CT (2014), 3 descendants of its own
- K143223: CGBA-032A, Aquilion PRIME Self-Propelled Scan Base Kit for IVR-CT (2015), 2 descendants of its own
- K182223: Aquilion ONE Self-Propelled Scan Base Kit for IVR-CT, CGBA-034A (2018), 1 descendant of its own
- K251645: Self-Propelled CT Scan Base Kit, CGBA-035A; Alphenix, INFX-8000C/B, INFX-8000C/S, V9.6 with Calculated DAP (2025), 0 descendants of its own

## Indications for use
Optional movable gantry base unit for use with the Aquilion LB CT Scanner to support the longitudinal movement and allow the acquisition of images in the z-direction (Z-axis).

Source page: https://510kreport.com/device/K111633
Methodology: https://510kreport.com/methodology